This training course is another course oriented to the applicants of medical device registration after the initiation of eRPS system. To steadily promote eRPS system, Beijing Drug Administration and CAMDI, as required by the Center for Medical Device Evaluation, NMPA (CMDE), actively participated in the work, introduced the eRPS system and registration process with an open and sincere attitude and encouraged the electronic submission.
The eRPS system is established to implement the relevant policies set forth in the Opinions of the General Office of the CPC Central Committee and the General Office of the State Council on Deepening the Reform of the Review & Approval System to Encourage the Innovation of Drugs and Medical Devices, and to align the supervision with the international supervision mechanism emphasized by National Medical Products Administration (NMPA). The establishment and promotion of eRPS system will help promote the level of information of “Internet + Government Affairs Service”, save the circulation time of the medical device registration information, relieve the administrative counterpart of medical devices from the burdens of declaration, substantially improve the quality of administration information, and optimize the evaluation and approval. It aims to help the administrative counterpart to transit from paper information to electronic information in a fast and effective manner, and accomplish the submission smoothly and efficiently.
Nearly 300 domestic and foreign enterprises participated in the training course. The representatives listened carefully and asked question actively, and experts gave elaborations patiently. The place was under a congenial atmosphere. CAMDI will continue to collect the members’ demands and carry out targeted high quality training persistently to help enterprises solve the practical problems and improve industrial development.